The Ability to Monitor Lung Function From Home is Overwhelmingly Popular, Survey Finds
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The Ability to Monitor Lung Function From Home is Overwhelmingly Popular, Survey Finds

An online patient survey has found that 96% of pulmonary fibrosis patients, and 93% of cystic fibrosis patients, support being able to monitor their lung function at home between visits…

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The Role of Microbial Sequencing in Understanding the Causes of Airway Inflammatory Diseases
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The Role of Microbial Sequencing in Understanding the Causes of Airway Inflammatory Diseases

Researchers at Northern Arizona University (NAU) are using microbial sequencing to better understand the causes of airway inflammatory diseases, including chronic rhinosinutsitis and cystic fibrosis. They hope that by studying…

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A Potential Treatment for Pulmonary Infection in Cystic Fibrosis has Been Awarded Patent Status
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A Potential Treatment for Pulmonary Infection in Cystic Fibrosis has Been Awarded Patent Status

A potential treatment of pulmonary infection for patients with cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) has just been awarded U.S. patent status, reports Medicalxpress. Dr Daniel Hassett, a researcher…

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After Getting Access to a Life Saving Drug, a Canadian Woman With Cystic Fibrosis Wants the Same for Others
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After Getting Access to a Life Saving Drug, a Canadian Woman With Cystic Fibrosis Wants the Same for Others

According to a story from cbc.ca, Lilia Zaharieva, a woman from British Columbia with cystic fibrosis, was recently given long term access to a treatment that is currently saving her…

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Researchers Use New Method With Electronic Health Records To Identify Genetic Diseases
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Researchers Use New Method With Electronic Health Records To Identify Genetic Diseases

Vanderbilt University Medical Center researchers have discovered a new method of searching existing electronic medical records to help identify genetic diseases in larger populations, reported EurekAlert!. Many people who may…

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The FDA Gave Orphan Drug Designation to an Investigational Treatment For Cystic Fibrosis
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The FDA Gave Orphan Drug Designation to an Investigational Treatment For Cystic Fibrosis

According to a story from Financial Buzz, the pharmaceutical company Proteostasis Therapeutics recently announced that the company's experimental treatment PTI-428 was granted Orphan Drug Designation by the FDA. PTI-428 is…

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Inspired by Her Daughter, Mrs. South Africa Plans a Daring Climb to Promote Rare Disease Awareness
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Inspired by Her Daughter, Mrs. South Africa Plans a Daring Climb to Promote Rare Disease Awareness

According to a story from All4Women, Nicole Capper, crowned Mrs. South Africa, is planning to summit Mt. Everest, the highest mountain peak on the planet, in order to help promote…

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Multiple Rare Disease Drugs Just Got Limited Coverage in British Columbia
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Multiple Rare Disease Drugs Just Got Limited Coverage in British Columbia

According to a story from the Vancouver Sun, five rare disease drugs just received coverage in British Columbia. The funding comes from savings accumulated thanks to a recent agreement that…

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These Rare Disease Treatments Just Became a Lot More Affordable for Australians
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These Rare Disease Treatments Just Became a Lot More Affordable for Australians

The Australian government has announced that almost that new treatments worth $300 million are being added to the Pharmaceutical Benefits Scheme. This program provides subsidized medical treatments to citizens of…

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Why Are US Children with Cystic Fibrosis Improving Faster than Canadian Kids?
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Why Are US Children with Cystic Fibrosis Improving Faster than Canadian Kids?

Why are US children with cystic fibrosis improving faster than Canadian kids? Newborn screenings and child healthcare programs may be behind the improvement among US children with cystic fibrosis. There's…

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